Ace Therapeutics offers specialized Air-Liquid Interface (ALI) culture services designed to advance your respiratory preclinical research. Our in vitro models recapitulate key features of human airways, including mucociliary differentiation, barrier function, and innate immune responses. Whether you are investigating asthma, COPD, pulmonary fibrosis, or respiratory infections, our customizable ALI platforms provide a robust tool for efficacy testing, toxicity assessment, and mechanistic studies.
Our service portfolio covers the entire workflow of ALI-based investigations. The table below outlines our core capabilities:
| Service Component | Example Applications / Deliverables |
| ALI Model Establishment | |
| Treatment & Intervention | |
| Endpoint Analysis & Functional Readouts |
Our custom ALI models serve as versatile platforms for a wide range of preclinical applications:
We recognize that every research question is unique. Our scientists work closely with you to tailor every aspect of the study. Whether you require a simple model for screening or a complex, multi-cell system for mechanistic deep-dives, we design the protocol, treatment regimen, and analytical endpoints to deliver the precise data you need.
Contact our team today to discuss how our Air-Liquid Interface (ALI) culture services can accelerate your preclinical respiratory program. We are committed to providing the scientific partnership and technical excellence you need to make informed decisions.
What cell sources are available for ALI cultures at Ace Therapeutics?
Ace Therapeutics offers a variety of cell types including primary human bronchial/tracheal epithelial cells (normal and diseased), small airway epithelial cells, and iPSC-derived airway progenitors. We can also work with cells isolated from patient samples or genetically modified lines provided by you, per your requirements.
Can you develop ALI models that mimic specific respiratory diseases?
Yes, we specialize in disease-relevant ALI models. For instance, we can establish cultures from COPD or asthma patients, or introduce specific genetic mutations (e.g., CFTR, SFTPC) to model cystic fibrosis or pulmonary fibrosis. Additionally, controlled exposure to inflammatory stimuli (e.g., IL-13) or cigarette smoke extract can recapitulate disease-like phenotypes in healthy cells.
What types of analyses can be performed on ALI cultures post-treatment?
Our downstream analysis portfolio is extensive. It includes assessment of barrier integrity (TEER, permeability), ciliary function (high-speed video microscopy), mucus production (ELISA, histochemistry), cytokine/chemokine profiling (multiplex immunoassays), gene expression (qPCR, RNA-seq), protein expression (Western blot, proteomics), and structural analysis by histology or electron microscopy. We tailor the endpoint selection to your specific study objectives.
How do you ensure consistency and reproducibility of ALI cultures?
We adhere to rigorous quality control measures. All cells are sourced from accredited vendors or carefully characterized in-house. Culture conditions are standardized, and differentiation is meticulously monitored by microscopy and functional markers (e.g., cilia, tight junctions). Each study includes appropriate controls, and we provide detailed documentation of culture performance and raw data for full transparency.
Do you offer co-culture models with other cell types (e.g., endothelial or immune cells)?
Absolutely. To better mimic the complex airway microenvironment, we can develop ALI co-cultures incorporating fibroblasts, endothelial cells, or macrophages (e.g., THP-1 or primary). These advanced models enable the investigation of cell-cell interactions in inflammation, fibrosis, or drug response.
What information do you need to provide a quote for ALI study services?
To prepare a customized proposal, please share your research objectives, preferred cell types, details of the treatment or intervention, desired endpoints, and any specific requirements (e.g., co-cultures, exposure systems). Our scientific team will then design a study plan and provide a detailed cost estimate and proposed timeline for your review.
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